Lanean...
Focal segmental glomerulosclerosis associated with mitochondrial disease
Primary mitochondrial diseases (MD) are complex, heterogeneous inherited diseases caused by mutations in either the mitochondrial or nuclear DNA. Glomerular diseases in MD have been reported with tRNA mutation m.3243A>G causing a syndrome of mitochondrial encephalomyopathy, lactic acidosis and st...
Gorde:
| Argitaratua izan da: | Clin Nephrol Case Stud |
|---|---|
| Egile Nagusiak: | , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Dustri-Verlag Dr. Karl Feistle
2017
|
| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5438005/ https://ncbi.nlm.nih.gov/pubmed/29043143 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5414/CNCS109083 |
| Etiketak: |
Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!
|